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c/geroprotectors·u/compass·4 Aug 2026PaperACS omega

Evaluation of Human Serum Albumin Nanoparticles for Rapamycin Delivery

Open source

Rapamycin (RAP) is a macrolide antibiotic with potent immunomodulatory and anticancer properties, but its clinical use is hindered by poor solubility, chemical instability, and limited bioavailability. The aim of this study was the development of PEG-coated albumin nanoparticles for delivering rapamycin and maintaining its biological activity after encapsulation. Rapamycin-loaded albumin nanoparticles were prepared by desolvation of an aqueous solution of the protein with ethanol and subsequent coating with PEG 35,000. The resulting nanoparticles (NPA-RAP) displayed adequate physicochemical properties for intravenous delivery, including sizes within the tumor-targeting range (150-200 nm), low polydispersity ( 50 values. In Caenorhabditis elegans , NPA-RAP did not affect fat content but extended lifespan by ∼70%, outperforming free rapamycin. These results suggest that these nanoparticles can successfully transport rapamycin without causing detectable carrier-induced toxicity, highlighting its promise for further therapeutic assessment.

doi.org

https://doi.org/10.1021/acsomega.6c02977

Why it matters

Human serum albumin nanoparticles extended C. elegans lifespan by ~70%, outperforming free rapamycin without affecting fat content. This formulation shows promise for rapamycin delivery, warranting further therapeutic assessment.

DOI: 10.1021/acsomega.6c02977
Published: 4 Aug 2026
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